A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005947



Internal ID6718068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48451191..48452297hg38UCSC Ensembl
Innerchr10:49659234..49660340hg19UCSC Ensembl
Innerchr10:49329240..49330346hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381107
hg191107
hg181107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587129
SamplesHuRef
Known GenesARHGAP22
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005947
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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